Canonical Allele Identifier: CA403081520
Gene: MCOLN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7526861A>C , CM000681.2:g.7526861A>C GRCh38
NC_000019.9:g.7591747A>C , CM000681.1:g.7591747A>C GRCh37
NC_000019.8:g.7497747A>C NCBI36
NG_015806.1:g.9252A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.506A>C MANE Select ENSP00000264079.5:p.Tyr169Ser
ENST00000264079.10:c.506A>C ENSP00000264079.5:p.Tyr169Ser
ENST00000394321.9:n.586A>C
ENST00000596008.1:n.468A>C
ENST00000598406.1:n.327A>C
ENST00000601003.1:c.506A>C ENSP00000469074.1:p.Tyr169Ser
NM_020533.2:c.506A>C NP_065394.1:p.Tyr169Ser
NM_020533.3:c.506A>C MANE Select NP_065394.1:p.Tyr169Ser